Kavitha Madheswaran

Kavitha Madheswaran has five years of work experience in the medical and healthcare industry. In 2021, they began working as the QA & RA Manager for HD Medical Group. Prior to that, in 2020, they worked as a Regulatory Affairs Consultant. From 2018-2017, they were a Senior Quality and Regulatory Analyst for HCL Technologies, where they were experienced in MDR transition, EU market Medical devices regulation, ISO 13485 and ISO 14971. From 2017-2015, they were a Research Assistant for Defense Research and Development Laboratory. Finally, from 2015-2017, they worked as a Biomedical Engineer for Clearmedi Healthcare Pvt. Ltd., where they were responsible for maintenance of digital linear accelerator, CAPA and tool maintenance activity.

Kavitha Madheswaran has a diverse educational background. Kavitha obtained their Higher Secondary Education from Adarsh Vidhyalaya HSS in 2008-2010, majoring in Maths and Biology. Kavitha then went on to pursue a Bachelor's degree in Bioengineering and Biomedical Engineering from College of Engineering, Guindy, which they completed in 2014. In 2016-2018, they completed a Master's degree in Biomedical/Medical Engineering from the same college. In 2018, they completed an Honors programme in Brain sciences and Bio imaging from Taipei Medical University. Additionally, they have obtained certifications in How to Maintain a QMS Compliant to MDR & IVDR from Greenlight Guru in 2021, European Medical device regulation from Tuv Sud South Asia PrivateLimited in 2020, Six Sigma Green Belt from AU-TVS, Anna University in 2013, and an Internship at Global Hospitals and Sri Ramakrishna Medical Centre, Chennai.